Thyroid hemiagenesis with Graves' disease: The first reported case in Lebanon

Mohamad Fleifel , Dana El Masri , Andrew El Alam , Gaby Khoury , Nouhad Genadry , Kamal Hirbli
{"title":"Thyroid hemiagenesis with Graves' disease: The first reported case in Lebanon","authors":"Mohamad Fleifel ,&nbsp;Dana El Masri ,&nbsp;Andrew El Alam ,&nbsp;Gaby Khoury ,&nbsp;Nouhad Genadry ,&nbsp;Kamal Hirbli","doi":"10.1016/j.jecr.2022.100128","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>Thyroid hemiagenesis (TH) is a rare disorder that is usually clinically silent unless associated with other thyroidal pathologies. We present a case of a TH patient with Graves' disease (GD). To our knowledge, this is the first ever case to be reported in Lebanon, and worldwide since 2017.</p></div><div><h3>Case Report</h3><p>A 45-years-old woman with GD was investigated for persistent anxiety and tremors. Radiological imaging disclosed the absence of the left thyroid lobe on neck ultrasound along with increased tracer uptake by the right lobe on the thyroid scan, in keeping with toxic right hemithyroid. This is an extremely rare case of thyroid hemiagenesis associated with Graves' disease (THGD).</p></div><div><h3>Discussion</h3><p>Clinical examination can help in the diagnosis of TH with the palpation of one thyroid lobe in the presence or absence of an isthmus. However to diagnose THGD, workup requires biochemical testing along with imaging and scintigraphy to compliment the findings of GD in the present lobe. Follow-up visits are very important to make sure that the treatment of choice has been effective and that there has not been any relapse.</p></div><div><h3>Conclusion</h3><p>THGD is a rare form of thyroid disorders that can be misdiagnosed sometimes. The actual pathophysiology of the disease is still unknown.</p></div>","PeriodicalId":56186,"journal":{"name":"Journal of Clinical and Translational Endocrinology: Case Reports","volume":"26 ","pages":"Article 100128"},"PeriodicalIF":0.0000,"publicationDate":"2022-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2214624522000223/pdfft?md5=4ccffab296f6bc7fffe3d66ca43865d7&pid=1-s2.0-S2214624522000223-main.pdf","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical and Translational Endocrinology: Case Reports","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2214624522000223","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

Background

Thyroid hemiagenesis (TH) is a rare disorder that is usually clinically silent unless associated with other thyroidal pathologies. We present a case of a TH patient with Graves' disease (GD). To our knowledge, this is the first ever case to be reported in Lebanon, and worldwide since 2017.

Case Report

A 45-years-old woman with GD was investigated for persistent anxiety and tremors. Radiological imaging disclosed the absence of the left thyroid lobe on neck ultrasound along with increased tracer uptake by the right lobe on the thyroid scan, in keeping with toxic right hemithyroid. This is an extremely rare case of thyroid hemiagenesis associated with Graves' disease (THGD).

Discussion

Clinical examination can help in the diagnosis of TH with the palpation of one thyroid lobe in the presence or absence of an isthmus. However to diagnose THGD, workup requires biochemical testing along with imaging and scintigraphy to compliment the findings of GD in the present lobe. Follow-up visits are very important to make sure that the treatment of choice has been effective and that there has not been any relapse.

Conclusion

THGD is a rare form of thyroid disorders that can be misdiagnosed sometimes. The actual pathophysiology of the disease is still unknown.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
甲状腺功能不全伴格雷夫斯病:黎巴嫩首例报道病例
背景:甲状腺功能不全(TH)是一种罕见的疾病,通常临床表现不明显,除非伴有其他甲状腺病变。我们报告一例TH患者合并Graves病(GD)。据我们所知,这是黎巴嫩乃至全球自2017年以来报告的第一例病例。病例报告:一名45岁的GD女性因持续焦虑和震颤而被调查。影像学显示颈部超声显示左甲状腺叶缺失,同时甲状腺扫描显示右甲状腺叶示踪剂摄取增加,与右甲状腺毒性相符。这是一个极其罕见的病例甲状腺功能不全与格雷夫斯病(THGD)。临床检查可以帮助诊断TH与触诊一个甲状腺叶在存在或不存在峡部。然而,为了诊断THGD,需要生化检查以及影像学和显像来补充本叶GD的发现。随访是非常重要的,以确保所选择的治疗是有效的,没有任何复发。结论thgd是一种罕见的甲状腺疾病,极易误诊。该疾病的实际病理生理机制尚不清楚。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Journal of Clinical and Translational Endocrinology: Case Reports
Journal of Clinical and Translational Endocrinology: Case Reports Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
1.10
自引率
0.00%
发文量
32
审稿时长
27 weeks
期刊介绍: The journal publishes case reports in a variety of disciplines in endocrinology, including diabetes, metabolic bone disease and osteoporosis, thyroid disease, pituitary and lipid disorders. Journal of Clinical & Translational Endocrinology Case Reports is an open access publication.
期刊最新文献
A case report of hypogonadism and infertility in 46,XX (SRY positive) male syndrome Severe hepatopulmonary syndrome with end-stage liver cirrhosis associated with pan-hypopituitarism in a pediatric patient A case of bone pain following kidney transplant: Differentiating between tertiary hyperparathyroidism and calcineurin-induced pain syndrome in post renal transplant patients Management of “hyperandrogenism” confounded by dermatology biotin prescriptions “Incidental” lipoadenoma of the parathyroid gland: A case report of a rare entity
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1